| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:23579231-23579383 | Common:3; Rare:46 | ||||
| chr13:24160500-24160821 | Common:1; Rare:88 | ||||
| chr13:24512739-24512836 | Common:2; Rare:30 | ||||
| chr13:26221791-26221953 | Rare:46 | ||||
| chr13:27251222-27251605 | Common:7; Rare:121 | ||||
| chr13:27424517-27424730 | Common:2; Rare:68 | ||||
| chr13:27450130-27450230 | Common:3; Rare:29 | ||||
| chr13:27450377-27450685 | Common:4; Rare:115 | ||||
| chr13:27620443-27620828 | Common:2; Rare:128 | ||||
| chr13:27919831-27920031 | Common:1; Rare:56 | ||||
| chr13:28659071-28659184 | Rare:48; Clinvar (pathogenic):1 | ||||
| chr13:30307007-30307211 | Common:4; Rare:49 | ||||
| chr13:30307390-30307479 | Common:2; Rare:35 | ||||
| chr13:30617565-30618039 | Common:1; Rare:147 | ||||
| chr13:32031564-32031792 | Common:1; Rare:67 |